Xueliang Kang

Enhanced photocatalytic performances of CeO2/TiO2 nanobelt heterostructures.

CeO2 /TiO2 nanobelt heterostructures are synthesized via a cost-effective hydrothermal method. The as-prepared nanocomposites consist of CeO2 nanoparticles assembled on the rough surface of TiO2 nanobelts. In comparison with P25 TiO2 colloids, surface-coarsened TiO2 nanobelts, and CeO2 nanoparticles, the CeO2 /TiO2 nanobelt heterostructures exhibit a markedly enhanced photocatalytic activity in the degradation of organic pollutants such as methyl orange (MO) under either UV or visible light irradiation. The enhanced photocatalytic performance is attributed to a novel capture-photodegradation-release mechanism. During the photocatalytic process, MO molecules are captured by CeO2 nanoparticles, degraded by photogenerated free radicals, and then released to the solution. With its high degradation efficiency, broad active light wavelength, and good stability, the CeO2 /TiO2 nanobelt heterostructures represent a new effective photocatalyst that is low-cost, recyclable, and will have wide application in photodegradation of various organic pollutants. The new capture-photodegradation-release mechanism for improved photocatalysis properties is of importance in the rational design and synthesis of new photocatalysts.

UV-visible-light-activated photocatalysts based on Bi2O3/Bi4Ti3O12/TiO2 double-heterostructured TiO2 nanobelts

Surface engineering of TiO2 nanobelts by the controlled assembly of functional heterostructures represents an effective approach for the synthesis of high-performance photocatalysts. In this study, we prepared a novel Bi2O3/Bi4Ti3O12/TiO2 double-heterostructured nanobelt by depositing bismuth hydroxide onto the TiO2 nanobelt surface. A thermal annealing treatment led to the formation of a Bi4Ti3O12 interlayer that functioned as a bridge to link Bi2O3 and TiO2. The double-heterostructured TiO2 nanobelts exhibited better UV light photocatalytic performance than commercial P25. Importantly, the photocatalytic activity in the visible range was markedly better than that of Bi2O3 and Bi2O3/TiO2 heterostructured TiO2 nanobelts. The enhanced performance was accounted for by the material band structures where the matching was improved by the unique interlayer.

Cr(VI), Pb(II), Cd(II) adsorption properties of nanostructured BiOBr microspheres and their application in a continuous filtering removal device for heavy metal ions

Uniform well-defined nanostructured BiOBr microspheres have been fabricated via a simple hydrothermal method in the presence of cetyltrimethylammonium bromide (CTAB) and ethylene glycol (EG). The heavy metal ion adsorption on the as-synthesized nanostructured BiOBr microspheres was systematically assessed by measuring the residual concentration during the adsorption process using a colorimetric method for Cr(VI) concentration, and an extraction-colorimetric method for Cd(II) and Pb(II) concentrations. The nanostructured BiOBr microspheres showed good removal capacity for heavy metal ions (Cr, Cd, Pb), and excellent adsorption properties for low concentration heavy metal ions, indicating potential applications in water purification. Based on the quick and efficient heavy metal ion removal ability of nanostructured BiOBr microspheres, a continuous filtering-type water purification device was designed and constructed. In using this continuous filtering type water purification device, 1 g of adsorbent can purify about 4900 g of Pb(II) contaminated water, 5900 g of Cd(II) contaminated water, or 21 500 g of Cr(VI) contaminated water having initial concentrations of 200 μg L−1 to successfully attain the World Health Organization standard for drinking water. The good removal capacity can be attributed to the hierarchical nanostructure, which displays a large specific surface area and strong adsorption of heavy metal ions.

High-Energy Faceted SnO2-Coated TiO2 Nanobelt Heterostructure for Near-Ambient Temperature-Responsive Ethanol Sensor

A SnO2 gas sensor was prepared by a two-step oxidation process whereby a Sn(II) precursor was partially oxidized by a hydrothermal process and the resulting Sn3O4 nanoplates were thermally oxidized to yield SnO2 nanoplates. The SnO2 sensor was selective and responsive toward ethanol at a temperature as low as 43 °C. This low sensing temperature stems from the rapid charge transport within SnO2 and from the presence of high-energy (001) facets available for oxygen chemisorption. SnO2/TiO2 nanobelt heterostructures were fabricated by a similar two-step process in which TiO2 nanobelts acted as support for the epitaxial growth of intermediate Sn3O4. At temperatures ranging from 43 to 276 °C, the response of these branched nanobelts is more than double the response of SnO2 for ethanol detection. Our observations demonstrate the potential of low-cost SnO2-based sensors with controlled morphology and reactive facets for detecting gases around room temperature.

One-Dimensional Ferroelectric Nanostructures: Synthesis, Properties, and Applications

One‐dimensional (1D) ferroelectric nanostructures, such as nanowires, nanorods, nanotubes, nanobelts, and nanofibers, have been studied with increasing intensity in recent years. Because of their excellent ferroelectric, ferroelastic, pyroelectric, piezoelectric, inverse piezoelectric, ferroelectric‐photovoltaic (FE‐PV), and other unique physical properties, 1D ferroelectric nanostructures have been widely used in energy‐harvesting devices, nonvolatile random access memory applications, nanoelectromechanical systems, advanced sensors, FE‐PV devices, and photocatalysis mechanisms. This review summarizes the current state of 1D ferroelectric nanostructures and provides an overview of the synthesis methods, properties, and practical applications of 1D nanostructures. Finally, the prospects for future investigations are outlined.

Nd:MgO:LiTaO3 crystal for self-doubling laser applications: growth, structure, thermal and laser properties

Nd3+ and Mg2+ co-doped LiTaO3 (Nd:MgO:LT) crystal has great potential for applications in self-frequency doubling (SFD) lasers, and self-optical parametric oscillation (SOPO) infrared lasers. However, a related high performance laser device has not yet been realized. No reliable data on the basic physical properties of Nd:MgO:LT have been obtained, because of the lack of high quality Nd:MgO:LT crystals available due to the great difficulty in growing this crystal. In this paper, by optimizing the growth parameters and the thermal field by means of simulation, a high quality Nd3+ and Mg2+ co-doped LiTaO3 crystal was grown by a modified Czochralski method. A comprehensive characterization of the crystal, including structure, composition, thermal properties, and CW laser performance, was performed. The experimental results indicate that Nd:MgO:LT is a monocrystal with strong anisotropic physical properties. The anisotropic thermal expansion was confirmed by observing the lattice parameter variation via temperature-dependent XRD analysis. Some important physical property data, such as thermal diffusivity, thermal conductivity and specific heat of the Nd:MgO:LT single crystal are reported for the first time, and should be of great utility for the application of this crystal. A CW laser output power of 3.58 W with an optical-to-optical conversion efficiency of 11.55, and a slope efficiency of 13.78%, was achieved with an incident pump power of 31 W, which is the highest laser output reported for this kind of crystal. It is demonstrated that single crystal Nd:MgO:LT will have important applications in SFD and SOPO lasers.

High output power of differently cut Nd:MgO:LiTaO3 CW lasers

A high-quality Nd3+ and Mg2+ co-doped LiTaO3 (Nd:MgO:LT) crystal was grown by the Czochralski method. The polarized absorption spectra and fluorescence spectra were studied, and the absorption cross section was calculated by Judd–Ofelt (J–O) theory. The laser performance with different sample cuts of the crystal was investigated for the first time, and it was found that Nd:MgO:LT crystal with different cutting directions (a and c) exhibits different laser properties. By optimizing a partial reflectivity mirror in the laser experimental setting, a high continuous wave output power of 3.58 W was obtained at 1092 and 1076 nm with an optical-to-optical conversion efficiency of 22.78% and slope efficiency of 26.06%. The results indicate that Nd:MgO:LT crystal is a promising candidate for the manufacture of Nd3+ doped periodically poled MgO:LiTaO3 crystal (Nd:PPMgOLT), which should have considerable applications in self-frequency doubling and optical parametric oscillation laser devices.

Introducing kalium into copper sulfide for the enhancement of thermoelectric properties

Advanced thermoelectric technology offers the potential to convert waste heat into useful electricity, and a mechanism of transmission-free methods for solid state cooling. A low thermal conductivity is a prerequisite for obtaining high efficiency thermoelectric materials. It is a challenge to achieve low thermal conductivity without simultaneously destroying the electric conductivity, for which a ‘phonon glass/liquid–electron crystal’ is proposed. To realize the phonon glass–electron crystal, a host–guest cage crystal system is considered, while to realize the phonon liquid–electron crystal, superionic conductivity is needed. Here we report a novel material, a KCu7−xS4 nanowire, which exhibits enhanced thermoelectric properties compared to the traditional chalcogenide Cu7S4 nanostructure. The presence of K ions not only forms a clathrate and a superionic fluid structure, which provides the phonon glass and liquid–electron crystal, but also adjusts the product to give a nanowire-like morphology. A low thermal conductivity and large Seebeck coefficient can be achieved when the nanowires are pressed into a bulk material. Higher electrical conductivity is also obtained below 420 K. In addition, the numerous grain boundaries, Cu deficiency and the orientated nanowires further increase the thermoelectric properties. The results indicate a new strategy to obtain high efficiency thermoelectric materials by introducing kalium into copper chalcogenides to form a new crystal structure with ‘phonon glass and liquid–electron crystal’ properties.

Formation mechanism and elimination methods for anti-site defects in LiNbO3/LiTaO3 crystals

Lithium niobate (LiNbO3 or LN) and lithium tantalate (LiTaO3 or LT) crystals, which have been widely applied in many fields such as electro-optics, birefringence, nonlinear optics, photorefraction, piezoelectricity and other areas, are reviewed. The studies of the properties and growth techniques are reviewed to give a brief idea of the growth of LN and LT crystals with high quality. The anti-site defects of these crystal materials have been accepted as one of the key factors constraining the improvement of their properties. This review shows the simulated calculation and structure of anti-site defects in LN/LT crystals and their effect on the physical properties and summarizes the recent progress in theoretical and technical processes, including the improved applications. We reviewed two main methods for the elimination of anti-site defects: doping of metal ions and growth of stoichiometric crystals. Finally, the prospects for future studies are outlined.

Antisite defect elimination through Mg doping in stoichiometric lithium tantalate powder synthesized via a wet-chemical spray-drying method

MgO-doped stoichiometric LiTaO3 (MgO:SLT) is one of the most promising nonlinear materials. However, its industrial application is limited by the poor optical quality caused by the nonhomogeneous distribution of magnesium. Herein, an MgO:SLT polycrystalline powder was synthesized with a homogenous magnesium distribution by a wet-chemical spray-drying method. A comparative investigation of the coordination state of Ta ions in MgO:SLT powders synthesized by this method and by a conventional solid-state reaction method was performed by X-ray photoelectron spectroscopy. It is proved that the Ta–Li antisite was completely eliminated as a result of the homogeneous Mg doping in the SLT lattice using the wet-chemical spray-drying method. However, for MgO:LT powder produced by the solid-state reaction method, element analysis after acid treatment shows that some Mg ions did not enter the LT lattice after high-temperature calcination. Also, scanning electron microscopy and transmission electron microscopy energy dispersive spectroscopy verified that some MgO particles still exist in the as-synthesized MgO:LT powder. This synthesis method can be used for mass production of high-quality polycrystalline powders for doped crystal growth and some other doped oxide powder products with high melt point.